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Nature Medicine|February 6, 2010
Straight talk with...Ken Getz. [Interviewed by Cassandra Willyard]Ken GetzExpert Review of Clinical Pharmacology|May 4, 2019
Assessing the adoption of clinical trial results summary disclosure to patients and the publicKen Getz, Julia Farides-MitchellClinical Therapeutics|July 17, 2019
Using Patient Advisory Boards to Solicit Input Into Clinical Trial Design and ExecutionAnnick Anderson, Jasmine Benger, Ken GetzHuman Vaccines & Immunotherapeutics|April 13, 2026
Quantifying vaccine dissemination for uptake comparisons between vaccinesAbigail Dirks, Hana Do, Madison Ford, et al.Academic Medicine : Journal of the Association of American Medical Colleges|July 27, 2006
Variability in the costs of institutional review board oversightMargaret M Byrne, Jeanne Speckman, Ken Getz, et al.Therapeutic Innovation & Regulatory Science|September 20, 2018
Benchmarking the Study Initiation ProcessMary Jo Lamberti, Cindy Brothers, Dan Manak, et al.Therapeutic Innovation & Regulatory Science|September 14, 2020
Evolving Clinical Data Strategies and Tactics in Response to Digital TransformationBeth Harper, Michael Wilkinson, Raj Indupuri, et al.Therapeutic Innovation & Regulatory Science|May 2, 2018
Baseline Assessment of the Evolving 2017 eClinical LandscapeMichael Wilkinson, Richard Young, Beth Harper, et al.Therapeutic Innovation & Regulatory Science|February 3, 2020
Assessing Outsourcing Oversight Practices and PerformanceMichael Wilkinson, Beth Harper, Julie Peacock, et al.Therapeutic Innovation & Regulatory Science|May 2, 2018
Assessing Study Start-up Practices, Performance, and Perceptions Among Sponsors and Contract Research OrganizationsMary Jo Lamberti, Michael Wilkinson, Beth Harper, et al.Pageof 2